Home Chemistry Heterocyclic Building Blocks Pyrimidines 2-Chloro-5-Nitropyrimidine
Nucleophilic Substitution (SN) Reactions: The chlorine atom at the 2-position can undergo nucleophilic substitution reactions with nucleophiles (such as amines or thiolates) to replace the chlorine with a new substituent.
Reduction Reactions: The nitro group (-NO2) is reducible, and the compound may undergo reduction reactions to form the corresponding amino compound. Common reducing agents include metal catalysts (e.g., palladium on carbon) or hydrogen gas.
Metalation Reactions: The 2-chloro-5-nitropyrimidine might undergo metalation reactions with strong bases, leading to the formation of an organometallic compound. This can subsequently be used in various synthetic transformations.
Arylation Reactions: The 2-chloro-5-nitropyrimidine can participate in palladium-catalyzed coupling reactions (such as Suzuki-Miyaura coupling) to form arylated derivatives.
Substitution Reactions: The compound may undergo substitution reactions at the 5-nitro position, depending on the reaction conditions. For example, substitution with a nucleophile can occur at the nitro group.
Halogenation Reactions: The chloro substituent at the 2-position can undergo further halogenation reactions under appropriate conditions.
Nitration Reactions: The aromatic ring of the pyrimidine may undergo nitration reactions under specific conditions, introducing additional nitro groups.
Cyclization Reactions: The compound may undergo cyclization reactions under specific conditions, leading to the formation of fused ring systems or other cyclic structures.
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Ethyl 2,6-dichloro-5-nitropyrimidine-4-carboxylate
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2-Chloro-N-isopropyl-5-nitropyrimidin-4-amine
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2,4-Dichloro-5-nitropyrimidine
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